Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Draeger Infinity Acute Care System (IACS) Monitoring Solution. Catalog Number Recalled by Draeger Medical, Inc. Due to The displayed value for the invasive blood pressure...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Draeger Medical, Inc. directly.
Affected Products
Draeger Infinity Acute Care System (IACS) Monitoring Solution. Catalog Number MS20783 (Infinity MCable-Dual Hemo) Physiological patient monitoring system.
Quantity: 260
Why Was This Recalled?
The displayed value for the invasive blood pressure measurement of the IACS was different than the actual patient values. Liquid ingress in the cable connection may cause inaccurate measurements. This can happen if the Dual Hemo MCable is used in a non-vertical position, a vertical position but upside down, or laying it on the floor or on the patient bed.
Where Was This Sold?
This product was distributed to 3 states: CA, IL, MA
About Draeger Medical, Inc.
Draeger Medical, Inc. has 78 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report